Results 171 to 180 of about 779,152 (196)

Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience. [PDF]

Front Genet
Li D, Liang L, Meng D, He S.
europepmc   +1 more source

Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening. [PDF]

Int J Mol Sci
Lachover-Roth I, Peretz S, Zoabi H, Harel E, Livshits L, Filon D, Levin C, Koren A.   +7 more
europepmc   +1 more source

Ancestry of the major long-range regulatory site of the α-globin genes in the Portuguese population with the common 3.7 kb α-thalassemia deletion. [PDF]

Mol Biol Rep
Pena R, Lopes P, Gaspar G, Miranda A, Faustino P.   +4 more
europepmc   +1 more source

Case Report: Acute hepatitis A virus infection presenting with direct antiglobulin test-negative autoimmune hemolytic anemia and α-thalassemia trait. [PDF]

F1000Res
Debbabi H, Chakroun E, Hassine H, Kchir H, Cherif D, Yacoub H, Maamouri N.   +6 more
europepmc   +1 more source

Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy.

Blood
Chappell ME, Breda L, Tricoli L, Guerra A, Jarocha D, Castruccio Castracani C, Papp TE, Tanaka N, Hamilton N, Triebwasser MP, Ghiaccio V, Fedorky MT, Gollomp KL, Bochenek V, Roche AM, Everett JK, Cook EJ, Bushman FD, Teawtrakul N, Glentis S, Kattamis A, Mui BL, Tam YK, Weissman D, Abdulmalik O, Parhiz H, Rivella S.   +26 more
europepmc   +1 more source

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Rapid and simultaneous detection of β- thalassemia point mutations by reverse hybridization strip assay among Egyptian patients

Journal of Biochemistry, Microbiology and Biotechnology, 2016
Thalassemia is a wide range hereditary disease with high incidence in Egypt along with the high frequency of consanguineous marriages. Investigation the heterogeneity, molecular basis, and natural history are the most effective methods to deal with the thalassemia to develop effective method for management and prevention including the prenatal ...
Osama Shalaan, Moustafa Sakr, Ahmed Daif, Khalil Elhalfawy   +3 more
openaire   +1 more source

β-Thalassemia

Genetics in Medicine, 2017
β-Thalassemia is caused by reduced (β +) or absent (β 0) synthesis of the β-globin chains of hemoglobin. Three clinical and hematological conditions of increasing severity are recognized: the β-thalassemia carrier state, thalassemia intermedia, and ...
Raffaella Origa, Origa Raffaella
exaly   +2 more sources

Structure and Conformational Dynamics of a Stacked Dimeric G-Quadruplex Formed by the Human CEB1 Minisatellite

Journal of the American Chemical Society, 2014
Brahim Heddi, Alain Nicolas, Anh Tuan Phan   +2 more
exaly  

The Yeast Pif1 Helicase Prevents Genomic Instability Caused by G-Quadruplex-Forming CEB1 Sequences In Vivo

PLoS Genetics, 2009
Judith Lopes, Jean-Baptiste Boulé, Aurèle Piazza   +2 more
exaly  

Meiotic Recombination and Flanking Marker Exchange at the Highly Unstable Human Minisatellite CEB1 (D2S90)

American Journal of Human Genetics, 2000
Jérôme Buard, A J Jeffreys
exaly